Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,491 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,491 in last 12 months

Showing 1996119980 of 28,355 recalls

Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Right Foot/30mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Steris Corporation

Recalled Item: OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due...

The Issue: STERIS has identified that the pivot pin assembly located on the table top...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Amerx Health Care Corp.

Recalled Item: Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz....

The Issue: Product did not meet specifications for Zinc Acetate (OOS).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Integra LifeSciences Corp.

Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...

The Issue: The affected K-wires do not meet specification requirements. Specifically,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Merz North America, Inc.

Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...

The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...

The Issue: It was discovered that the generator of the system could possibly terminate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...

The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Devicor Medical Products Inc

Recalled Item: Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009...

The Issue: A 10 Gauge needle, 9cm long was shipped in an 8 Gauge needle, 15 cm package.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Richard Wolf Medical Instruments Corp.

Recalled Item: Conical portio adapter (acorn) small & large are used for Recalled by...

The Issue: The distal end of the Conical portio adapter (acorn) is composed of a small...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...

The Issue: It was discovered that the generator of the system could possibly terminate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...

The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard ventilator- Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Comprehensive ventilator- Recalled by Carefusion 211 Inc dba Carefusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing